Inorganic-organic composite-treated zinc-plated steel sheet

ABSTRACT

The present invention provides an inorganic-organic composite-treated zinc-plated steel sheet whose treated coatings do not contain any chromium and which is excellent in corrosion resistance after degreasing, coating adhesion and electrodeposition coating performance.  
     The inorganic-organic composite-treated zinc-plated steel sheet, which is obtained by forming a zinc phosphate coating, in a coating weight of 0.3 to 5 g/m 2 , on the zinc-plated steel sheet surface and forming thereon a post-treatment coating, in a coating weight of 0.01 to 1 g/m 2 , by using a post-treatment composition containing at least one compound (A) selected from the group consisting of thiocarbonyl group-containing compounds, sulfide group-containing compounds and guanidyl group-containing compounds, an organic resin (B), a crosslinking agent (C) and an inorganic corrosion inhibitor (D).

TECHNICAL FIELD

This invention relates to an inorganic-organic composite-treatedzinc-plated steel sheet.

BACKGROUND ART

In the art, zinc-plated steel sheets intended for use in the fields ofautomobiles, household electric appliances, building materials and thelike are generally subjected to phosphate treatment or chromatetreatment for the purpose of improving their corrosion resistance andcoating adhesion, and the like. In particular, the process comprisingchromate sealing treatment following zinc phosphate treatment is in wideuse since it is highly effective in improving corrosion resistance andcoating adhesion. However, with the recent background of the increasinginterest in environmental problems, it is desired that a surfacetreatment technology without using any highly toxic chromate bedeveloped. Thus, the following technologies have been proposed.

A zinc phosphate composite-treated steel sheet has been disclosed whichhas, as a first layer on the zinc-plated steel sheet surface, a zincphosphate coating with a coating weight of 0.2 to 2.5 g/m² andcontaining at least one metal selected from among nickel, manganese andmagnesium and, thereon, as a second layer, an organic coating based onat least one organic resin selected from among ethylene resins, epoxyresins, urethane resins and acrylic resins (cf. e.g. Japanese KokaiPublication 2001-105528, page 2).

An organic composite-treated zinc-plated steel sheet has been disclosedwhich has a zinc plating coating, a zinc phosphate coating of not lessthan 0.3 g/m² and an organic coating of 0.3 to 2 g/m² as formed on thesteel sheet surface in that order, wherein the zinc phosphate coatingcontains Mg, the Mg/P ratio (by weight) in the zinc phosphate coating isnot less than 0.15 and the amount of Mg is not less than 20 mg/m² (cf.e.g. Japanese Kokai Publication 2001-131763, page 2).

The zinc-plated steel sheets treated in such a manner are generallypressed for shaping and then subjected to alkaline degreasing andwashing and are used either as such or after coating. In the automobilefield, in particular, the car bodies in which the zinc-plated steelsheets treated in the manner mentioned above are used are conveyed on acoating line and are thus subjected successively to alkaline degreasing,zinc phosphate treatment, electrodeposition coating, intermediatecoating, and top coating. Therefore, the coatings formed on thezinc-plated steel sheets are required to be firm and strong so that theymay not be dissolved or deteriorated even upon contact with an alkalinedegreasing solution and a zinc phosphate treatment solution.

However, when the zinc phosphate composite-treated steel sheets andorganic composite-treated zinc-plated steel sheets obtained by suchmethods as mentioned above and the like methods are subjected toalkaline degreasing treatment after shaping thereof, the coatings aredissolved or deteriorated, so that poor corrosion resistance after thedegreasing treatment and poor coating adhesion will result.

In view of the state of the art as discussed above, it is an object ofthe present invention to provide an inorganic-organic composite-treatedzinc-plated steel sheet whose treated coatings do not contain anyhazardous chromate and which is excellent in corrosion resistance afteralkaline degreasing and coating adhesion.

SUMMARY OF THE INVENTION

The present invention provides an inorganic-organic composite-treatedzinc-plated steel sheet

-   -   which has a zinc phosphate coating, in a coating weight of 0.3        to 5 g/m², on the zinc-plated steel sheet surface and, thereon,        a post-treatment coating, in a coating weight of 0.01 to 1 g/m²,        containing at least one compound (A) selected from the group        consisting of thiocarbonyl group-containing compounds, sulfide        group-containing compounds and guanidyl group-containing        compounds, an organic resin (B), a crosslinking agent (C) and an        inorganic corrosion inhibitor (D).

Said zinc phosphate coating preferably contains magnesium, themagnesium/phosphorus (weight ratio) in said zinc phosphate coating beingnot less than 0.1 and the amount of magnesium being not less than 20mg/m².

Said post-treatment coating preferably has the following composition:0.1 to 10% by weight of at least one compound (A) selected from thegroup consisting of thiocarbonyl group-containing compounds, sulfidegroup-containing compounds and guanidyl group-containing compounds, 40to 80% by weight of the organic resin (B), 5 to 30% by weight of thecrosslinking agent (C) and 10 to 40% by weight of the inorganiccorrosion inhibitor (D).

Said organic resin (B) preferably comprises a neutralizedethylene-unsaturated carboxylic acid copolymer (B1) and at least oneresin (B2) selected from the group consisting of acrylic resins,polyester resins, polyurethane resins and epoxy resins,

-   -   said copolymer (B1) preferably having a degree of neutralization        with an alkali metal of 30 to 90%,    -   said resin (B2) preferably having at least one functional group        selected from the group consisting of carboxyl, hydroxyl and        amide groups,    -   and the weight ratio between said copolymer (B1) and said resin        (B2) being preferably 100:0 to 20:80.

Said crosslinking agent (C) is preferably at least one species selectedfrom the group consisting of epoxy compounds, silane compounds, organictitanium compounds, amino resins, blocked isocyanate compounds andcarbodiimide compounds.

Said inorganic corrosion inhibitor (D) is preferably at least onespecies selected from the group consisting of silica particles,phosphoric acid compounds and niobium compounds.

DETAILED DESCRIPTION OF THE INVENTION

In the following, the present invention is described in detail.

The inorganic-organic composite-treated zinc-plated steel sheet of theinvention has, on the surface of the zinc-plated steel sheet, a zincphosphate coating and further thereon, a post-treatment coating. Thesetwo coatings which the sheet has contribute to improvements in corrosionresistance after alkaline degreasing and coating adhesion.

The inorganic-organic composite-treated zinc-plated steel sheet of theinvention has, on the surface of the zinc-plated steel sheet, a zincphosphate coating as a first coating. This coating can provide thezinc-plated steel sheet with certain extents of corrosion resistance,coating adhesion and lubricity.

The zinc phosphate coating can be formed by means of a per se known zincphosphating solution containing the phosphate ion and zinc ion.

The zinc ion resource is not particularly restricted but may be anyzinc-containing compound. For example, there may be mentioned zinc, zincoxide, zinc carbonate, zinc nitrate, and the like.

The phosphate ion resource is not particularly restricted but may be anyphosphoric moiety-containing compound. For example, there may bementioned phosphoric acid, phosphorus pentoxide, sodium dihydrogenphosphate, and the like. It may contain an appropriate amount of someother component used in the zinc phosphating solution.

The above-mentioned zinc phosphate coating preferably containsmagnesium. This can lead to a further improvement in corrosionresistance of the zinc-plated steel sheets and an improvement inadhesion to the post-treatment coating.

In cases where the zinc phosphate coating contains magnesium, thecoating preferably has a magnesium/phosphorus ratio in the coating(weight ratio between magnesium and phosphorus in the coating) of notless than 0.1. When the ratio is less than 0.1, the addition ofmagnesium may not result in a substantial improvement in corrosionresistance. A more preferred ratio is 0.15 to 0.5.

In cases where the zinc phosphate coating contains magnesium, the zincphosphate coating preferably has an amount of magnesium therein of notless than 20 mg/m². When the amount is less than 20 mg/m², noimprovement in corrosion resistance may possibly be achieved. Morepreferably, the amount is 30 to 70 mg/m².

The zinc phosphate coating is formed in a coating weight of from a lowerlimit of 0.3 g/m² to an upper limit of 5 g/m². When the coating weightis less than 0.3 g/m², unsatisfactory corrosion resistance may resultand, when it exceeds 5 g/m², coating peeling may occur upon severetreatment. The lower limit is more preferably 0.5 g/m², and the upperlimit is more preferably 2.5 g/m².

Usable as the treatment solution for forming the zinc phosphate coatingis a commercial treatment solution containing phosphate ions and zincions as main constituents, with metal ions other than zinc ions, nitrateions, fluoride ions and the like ions added according to need. Forincorporation of magnesium in the zinc phosphate coating, a bathresulting from addition of magnesium nitrate to the above zinc phosphatetreatment solution is judiciously used. The amount of magnesium and themagnesium/phosphorus ratio in the coating can be controlled through thelevel of addition of magnesium nitrate.

As regards the method of treating the zinc-plated steel sheet with theabove zinc phosphating solution, the zinc phosphate coating can beformed either in the manner of reaction type treatment or in the mannerof coating treatment. In the case of reaction type treatment, the zincphosphate coating can be formed, for example, by bringing thezinc-plated steel sheet after degreasing, water washing and surfaceconditioning into contact with the above zinc phosphate treatmentsolution, followed by washing with water and drying. The coating weightof the zinc phosphate coating can be adjusted by varying the treatmenttime and/or treatment temperature, for instance.

The coating type treatment comprises, for example, applying the zincphosphate treatment solution, in an amount corresponding to the requiredcoating weight, to the zinc-plated steel sheet by the roll coatingmethod, or applying the treatment solution to the steel sheet by dippingor spraying and then adjusting the coating weight to the required levelby roll squeezing. After application of the zinc phosphate treatmentsolution thereto, the treated zinc-plated steel plate is dried using adrying oven and the like whereby the zinc phosphate coating is formed.

The inorganic-organic composite-treated zinc-plated steel sheet of theinvention has, as a second coating formed on the above zinc phosphatecoating, a post-treatment coating containing at least one compound (A)selected from the group consisting of thiocarbonyl group-containingcompounds, sulfide group-containing compounds and guanidylgroup-containing compounds, an organic resin (B), a crosslinking agent(C) and an inorganic corrosion inhibitor (D). The formation of thepost-treatment coating on the above zinc phosphate coating results inimprovements in corrosion resistance after alkaline degreasing andcoating adhesion.

Thus, zinc-plated steel sheets with the zinc phosphate coating aloneformed thereon may have sites devoid of the compact zinc phosphatecoating on the steel sheet surface, leading to poor corrosionresistance. When zinc-plated steel sheets having only an inorganiccoating, such as zinc phosphate, as formed thereon are coated, they mayshow an unsatisfactory degree of coating adhesion in adhesion testingfollowing a bending or water resistance test. On the contrary, theinorganic-organic composite-treated zinc-plated steel sheet of theinvention has a further post-treatment coating formed on the zincphosphate coating and containing at least one compound (A) selected fromthe group consisting of thiocarbonyl group-containing compounds, sulfidegroup-containing compounds and guanidyl group-containing compounds, anorganic resin (B), a crosslinking agent (C) and an inorganic corrosioninhibitor (D) and, in this manner, the whole surface of the steel sheet,inclusive of those sites on which there are devoid of the compact zincphosphate coating, is covered uniformly with a firm and strong coating.Therefore, even after further shaping and alkaline degreasing treatmentthereof, the inorganic-organic composite-treated zinc-plated steel sheetof the invention is prevented from its post-treatment coating formedbeing deteriorated or dissolved upon degreasing treatment and, as aresult, good corrosion resistance after degreasing and coating adhesioncan be obtained.

The post-treatment coating can be formed by using a post-treatmentcomposition containing at least one compound (A) selected from the groupconsisting of thiocarbonyl group-containing compounds, sulfidegroup-containing compounds and guanidyl group-containing compounds, anorganic resin (B), a crosslinking agent (C) and an inorganic corrosioninhibitor (D).

The thiocarbonyl group-containing compounds, sulfide group-containingcompounds and guanidyl group-containing compounds mentioned above havehigh levels of affinity for the zinc ion and are therefore effective inpreventing zinc-coated steel sheets from becoming covered with whiterust.

The thiocarbonyl group-containing compounds are preferably onesrepresented by the general formula (1) given below. They can improve thecorrosion resistance of the zinc-plated steel sheet.

In the above formula, X and Y are the same or different and eachrepresents H, OH, SH or NH₂ or represents a hydrocarbon group containing1 to 15 carbon atoms which may have OH, SH or NH₂ as a substituent andmay contain —O—, —NH—, —S—, —CO—or —CS—; X and Y may be combined witheach other to form a ring.

The thiocarbonyl group-containing compounds represented by the generalformula (1) are compounds having the thiocarbonyl group of the followingformula (I):

and, among them, those compounds in which the thiocarbonyl group isbound to a nitrogen atom or oxygen atom represented by the followingformula (II):

A compound capable of forming a thiocarbonyl group-containing compoundin an aqueous solution or in the presence of an acid or alkali can alsobe used.

As examples of the thiocarbonyl group-containing compounds, there may bementioned thiourea represented by the following formula (III):

and derivatives thereof, for example methylthiourea, dimethylthiourea,trimethylthiourea, ethylthiourea, diethylthiourea, 1,3-dibutylthiourea,phenylthiourea, diphenylthiourea,1,3-bis(dimethylaminopropyl)-2-thiourea, ethylenethiourea,propylenethiourea, thiopental, thiocarbazide, thiocarbazones,thiocyanuric acids, thiohydantoin, 2-thiouracil, 3-thiourazole;thioamide compounds represented by the following formula (IV):

and derivatives thereof, for example thioformamide, thioacetamide,thiopropionamide, thiobenzamide, thiocarbostyril, thiosaccharin;thioaldehyde compounds represented by the following formula (V):

for example thioformaldehyde, thioacetaldehyde; carbothioic acidsrepresented by the following formula (VI):

and salts thereof; for example thioacetic acid, thiobenzoic acid,dithioacetic acid, sodium methyldithiocarbamate, sodiumdimethyldithiocarbamate, dimethyldithiocarbamic acid triethylamine salt,sodium diethyldithiocarbamate, pentamethylenedithiocarbamic acidpiperidine salt, pipecolyldithiocarbamic acid pipecoline salt, potassiumO-ethyl xanthate; thiocarbonic acids represented by the followingformula (VII):

for example, ethylene tridithiocarbonate; and other compounds having theabove structure (I), for example thiocoumazone, thiocoumothiazone,thionine blue J, thiopyrone, thiopyrine, thiobenzophenone and the like.These thiocarbonyl group-containing compounds may be used singly or twoor more of them may be used in combination. Among the thiocarbonylgroup-containing compounds mentioned above, those insoluble in water areeach once dissolved in an alkaline solution and then incorporated intothe post-treatment composition.

Preferably, the above thiocarbonyl group-containing compound is apolymer having a side chain represented by the general formula (2) givenbelow and a weight average molecular weight of not higher than1,000,000. When it is such a polymer, the zinc-plated steel sheet can bemore improved in corrosion resistance.

In the above formula, Z represents —(CH₂)_(a)COO-A in which a is aninteger of 1 to 8 and A represents ammonia, an amine or a univalentmetal ion.

The polymer having the side chain of general formula (2) is notparticularly restricted but there may be mentioned polymers representedby the general formula (3) given below.

In the above formula, m and n each is such an integer that the polymermay acquire a weight average molecular weight of not higher than1,000,000, with the ratio n/n+m of 0.2 to 0.8, preferably 0.3 to 0.6. Ifthis ratio is less than 0.2, the water solubility of the polymer willdecrease. Conversely, if it exceeds 0.8, the corrosion resistance willdecrease. The n A groups may be the same or different, and B and C eachrepresents a main chain of the polymer and may be, for example, a grouprepresented by the general formula (4) given below. Unless the sidechain binding position is specifically indicated in the general formula(4) given below, the side chain may be bound to any of the carbon atoms.The groups B and C may be the same or different.

The symbols p, q and r each represents an integer. Their values are notparticularly restricted provided that they cooperatively give a weightaverage molecular weight of not higher than 1,000,000 to the polymer.

Preferably, the thiocarbonyl group-containing compound is a polymerhaving a side chain represented by the above general formula (2) andhaving a weight average molecular weight of not higher than 1,000,000.When the molecular weight exceeds 1,000,000, the viscosity willincrease, possibly making it difficult to obtain uniform coatings.

The sulfide group-containing compound has the same effect as that of thethiocarbonyl group-containing compound. When it is contained in thepost-treatment coating, it can provide the thin film containing it withgood corrosion resistance.

The sulfide group-containing compound is not particularly restricted butmay be any sulfide group-containing compound. From the corrosionresistance viewpoint, however, a hydroxyl group-containing sulfidecompound is preferred.

The hydroxyl group-containing sulfide compound is not particularlyrestricted but may be any of hydroxyl group- and sulfidegroup-containing compounds, such as, for example,1,2-bis(2-hydroxyethylthio)ethane, 1,4-bis(2-hydroxyethylthio)butane,1,3-bis(2-hydroxyethylthio)-2-propanol,3-(2-aminophenylthio)-1,2-propanediol, sodium(2,3-dihydroxypropylthio)-2-methylpropanesulfonate, sodium(2,3-dihydroxypropylthio)propanesulfonate,3-(2-hydroxyethylthio)-2-hydroxypropylmercaptan, and3-(2-aminophenylthio)-2-hydroxypropylmercaptan.

The guanidyl group-containing compound has the same effect as that ofthe thiocarbonyl group-containing compound. When it is contained in thepost-treatment coating, it can provide the thin film containing it withgood corrosion resistance.

The guanidyl group-containing compound is not particularly restrictedbut may be any guanidyl group-containing compound. Preferred, however,are compounds represented by the formula (5) given below. These canimprove the corrosion resistance of the zinc-plated steel sheet.

In the above formula, X′ and Y′ may be the same or different and eachrepresents H, NH₂, a phenyl group or a methylphenyl (tolyl) group, ormay contain H, NH₂, a phenyl group or a methylphenyl (tolyl) group as asubstituent and, further, may contain —C(═NH)—, —CO—or —CS—.

As examples of the guanidyl group-containing compound, there may bementioned guanidine, aminoguanidine, guanylthiourea,1,3-di-o-tolylguanidine, 1-o-tolylbiguanide, 1,3-diphenylguanidine andthe like.

Such guanidyl group-containing compounds may be used singly or two ormore of them may be used in combination.

As regards the content of at least one compound (A) selected from thegroup consisting of the above-mentioned thiocarbonyl group-containingcompounds, sulfide group-containing compounds and guanidylgroup-containing compounds (the total content, in the post-treatmentcoating, of the thiocarbonyl group-containing compound, sulfidegroup-containing compound and/or guanidyl group-containing compoundselected), the lower limit thereto is preferably set at 0.1% by weight,and the upper limit is preferably set at 10% by weight. If the contentin question is lower than 0.1% by weight, the coating, when it is thin,may be unsatisfactory in corrosion resistance and, if it exceeds 10% byweight, the coating adhesion may decrease. The lower limit is morepreferably 0.2% by weight, and the upper limit is more preferably 5% byweight.

When the organic resin (B) is contained in the post-treatment coating,the post-treatment coating can be formed uniformly and at least onecompound (A) selected from the group consisting of the thiocarbonylgroup-containing compounds, sulfide group-containing compounds andguanidyl group-containing compounds and the inorganic corrosioninhibitor (D) can be appropriately fixed in the coating, and the topcoatadhesion can also be improved.

The organic resin (B) is not particularly restricted but may be anacrylic resin, vinyl resin, polyester resin, polyurethane resin, epoxyresin or the like, for instance. Preferably, it contains a neutralizedethylene-unsaturated carboxylic acid copolymer (B1) as an essentialcomponent because of the improvement in adhesion to the top coatingcomposition or electrodeposition coating composition as caused therebyand of the ability thereof to adequately fix at least one compound (A)selected from the group consisting of the thiocarbonyl group-containingcompounds, sulfide group-containing compounds and guanidylgroup-containing compounds and the inorganic corrosion inhibitor (D),which is to be more specifically described later herein, in the coating.

The ethylene-unsaturated carboxylic acid copolymer is a copolymerobtained by radical polymerization of ethylene and an unsaturatedcarboxylic acid such as methacrylic acid, acrylic acid, maleic acid,fumaric acid, itaconic acid or crotonic acid under high temperature andhigh pressure conditions.

The neutralized ethylene-unsaturated carboxylic acid copolymer (B1) isthe product of neutralization of a part of the carboxyl groups containedin the ethylene-unsaturated carboxylic acid copolymer with a basiccompound.

The neutralized ethylene-unsaturated carboxylic acid copolymer (B1) isthe product of neutralization with an alkali metal to a neutralizationdegree of 30 to 90%. Together with the alkali metal, ammonia and/or anorganic amine may be partly involved in the neutralization. Thus, theneutralization product (B1) is the product of neutralization of 30 to90% of the carboxyl groups contained in the ethylene-unsaturatedcarboxylic acid copolymer with an alkali metal supplied by a basicalkali metal compound, such as NaOH, KOH, RbOH or CsOH, with part or thewhole of the carboxyl groups remaining unneutralized with the alkalimetal being optionally neutralized with ammonia and/or an organic amine,if necessary.

The organic amine may be, for example, triethylamine, ethanolamine andthe like. Ammonia and such organic amines may be used singly or two ormore of them may be used in combination.

If the neutralized ethylene-unsaturated carboxylic acid copolymer (B1)has a degree of neutralization with the alkali metal compound of lessthan 30%, the coating may become low in firmness and strength, henceinsufficient in corrosion resistance. When the degree of neutralizationexceeds 90%, the coating may become low in water resistance, henceinsufficient in corrosion resistance.

In cases where the organic resin (B) comprises the neutralizedethylene-unsaturated carboxylic acid copolymer (B1), the neutralizedethylene-unsaturated carboxylic acid copolymer (B1) may be a modifiedone.

As the organic resin (B), there may be mentioned, in addition to theneutralized ethylene-unsaturated carboxylic acid copolymer (B1), acrylicresins, polyester resins, polyurethane resins, epoxy resins, and thelike. In cases where at least one resin (B2) selected from the groupconsisting of acrylic resins, polyester resins, polyurethane resins andepoxy resins is used as the organic resin (B), it is preferable that theresin (B2) have at least one functional group selected from the groupconsisting of carboxyl, hydroxyl and amide groups. Through suchfunctional groups, the resin (B2) reacts with the above-mentionedcrosslinking agent (C) to form a firm and strong coating. It is alsopossible to use the neutralized ethylene-unsaturated carboxylic acidcopolymer (B1) and the resin (B2) in combination to further improve thecoating adhesion.

When the organic resin (B) comprises the above-mentioned neutralizationproduct (B1) and resin (B2), the weight ratio (B1:B2) between theneutralization product (B1) and resin (B2) is preferably 100:0 to 20:80.If the neutralization product (B1) amounts to less than 20% by weightrelative to the total amount (100% by weight) of (B1) and (B2), any firmand strong coating may not be formed. More preferably, the ratio is100:0 to 30:70.

The content of the organic resin (B) in the post-treatment coating ispreferably 40% by weight (lower limit) to 80% by weight (upper limit) .When it is less than 40% by weight, any firm and strong coating may notbe formed; further, the coating adhesion may decrease. When it exceeds80% by weight, the corrosion resistance after alkaline degreasing maydecrease. The lower limit is more preferably 50% by weight, and theupper limit is more preferably 75% by weight.

By causing the crosslinking agent (C) to be contained in thepost-treatment composition, it becomes possible to improve the alkaliresistance and solvent resistance of the coating through the reaction ofthe crosslinking agent (C) with the functional groups in the organicresin (B), such as carboxylic and hydroxyl groups, for crosslinkformation.

The crosslinking agent (C) is not particularly restricted but may be anycompound having a plurality of reactive functional groups. From theviewpoint of firm and strong coating formation and improvements inalkali resistance and solvent resistance of the coating, it preferablycomprises at least one species selected from the group consisting ofepoxy compounds, silane compounds, organic titanium compounds, aminoresins, blocked isocyanates and carbodiimide compounds.

The epoxy compound is not particularly restricted but may be any ofthose compounds which have a plurality of oxirane rings, and there maybe mentioned, for example, adipic acid glycidyl ester, phthalic acidglycidyl ester, terephthalic acid glycidyl ester, sorbitol polyglycidylether, sorbitan polyglycidyl ether, polyglycerol polyglycidyl ether,pentaerythritol polyglycidyl ether, diglycerol polyglycidyl ether,glycerol polyglycidyl ether, trimethylpropane polyglycidyl ether,neopentyl glycol glycidyl ether, ethylene glycol diglycidyl ether,polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether,polypropylene glycol diglycidyl ether,2,2-bis(4′-glycidyloxyphenyl)propane, triglycidyltris(2-hydroxyethyl)isocyanurate, tris(2,3-epoxypropyl)isocyanurate,bisphenol A diglycidyl ether, hydrogenated bisphenol A diglycidyl ether,and like glycidyl group-containing compounds. These may be used singlyor two or more of them may be used in combination.

The silane compound is not particularly restricted but may be any ofthose silane compounds which have a plurality of reactive functionalgroups, and there may be mentioned, for example, vinyltrimethoxysilane,vinyltriethoxysilane, γ-aminopropltrimethoxysilane,γ-aminopropylethoxysilane,N-[2-(vinylbenzylamino)ethyl]-3-aminopropyltrimethoxysilane,γ-methacryloxypropylmethyldimethoxysilane,γ-methacryloxypropyltrimethoxysilane,γ-methacryloxypropylmethyldiethoxysilane,γ-methacryloxypropyltriethoxysilane, γ-glycidoxypropyltriethoxysilane,γ-glycidoxypropylmethyldiethoxysilane,γ-glycidoxypropyltrimethoxysilane,2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane,N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane,N-(β-aminoethyl)-γ-aminopropyltriethoxysilane,N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane,N-phenyl-γ-aminopropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilaneand the like. The above-mentioned silane compounds include the productsresulting from hydrolysis of the respective silanes. These may be usedsingly or two or more of them may be used in combination.

The organic titanium compound is not particularly restricted but may beany titanium-containing organic compound. Thus, there may be mentioned,for example, dipropoxybis(triethanolaminato)titanium,dipropoxybis(diethanolaminato)titanium,dibutoxybis(triethanolaminato)titanium,dibutoxybis(diethanolaminato)titanium,dipropoxybis(acetylacetonato)titanium,dibutoxybis(acetylacetonato)titanium, dihydroxybis(lactate)titaniummonoammonium salt, dihydroxybis (lactate) titanium diammonium salt,propanedioxytitanium bis(ethyl acetoacetate), oxotitaniumbis(monoammonium oxalate), isopropyl tri(N-amidoethylaminoethyl)titanate and the like. These may be used singly or two or more of themmay be used in combination.

The amino resin is not particularly restricted but there may bementioned, for example, methylolated amino resins obtained by reactingan amino component, such as melamine, urea, benzoguanamine,acetoguanamine, stearoguanamine or spiroguanamine, with formaldehyde ora formaldehyde source such as paraformaldehyde or trioxane, and thelike. The methylol group(s) of the above-mentioned methylolated aminoresins may be etherified with an alkyl group. These may be used singlyor two or more of them may be used in combination.

The blocked isocyanate compound is not particularly restricted but theremay be mentioned, for example, compounds resulting from blocking of theisocyanato groups of aliphatic, alicyclic or aromatic polyisocyanatecompounds with an active hydrogen-containing compound. As the activehydrogen-containing compound, there may be mentioned such compounds asphenols, alcohols, active methylene-containing compounds, oximes andnitrite salt compounds.

The above-mentioned carbodiimide compound is not particularly restrictedbut may be any of those obtained by decarboxylation condensation ofaliphatic diisocyanates, for instance.

The content of the crosslinking agent (C) is preferably 5% by weight(lower limit) to 30% by weight (upper limit) in the post-treatmentcoating. When it is less than 5% by weight, the organic resin (B) willbe crosslinked only to an insufficient extent, possibly resulting indecreases in alkali resistance and solvent resistance of the coatings.If it exceeds 30% by weight, the crosslinking agent becomes excessive,possibly resulting in a decrease in coating firmness and strength anddecreases in corrosion resistance and coating adhesion.

By causing the inorganic corrosion inhibitor (D) to be contained in thepost-treatment coating, it becomes possible to allow the formation of astable metal corrosion product in corrosive circumstances, whereby theprogress of corrosion can be prevented and the coatings can be providedwith good corrosion resistance.

The inorganic corrosion inhibitor (D) is not particularly restricted butmay be any inorganic compound having corrosion inhibitor effect. Fromthe higher corrosion inhibiting effect viewpoint, however, silicaparticles, phosphoric acid compounds and niobium compounds arepreferred.

The above-mentioned silica particles are not particularly restricted butfine silica particles with a primary particle diameter of 5 to 50 nm,for example colloidal silica, fumed silica, ion exchange silica and thelike, are preferred since the post-treatment coating is thin. Ascommercial products, there may be mentioned, for example, Snowtex O,Snowtex N, Snowtex C and Snowtex IPA-ST (Nissan Chemical Industries,Ltd.), Adelite AT-20N and AT-20A (Asahi Denka Co., Ltd.), Aerosil 200(Nippon Aerosil Co., Ltd) and the like.

The phosphoric acid compounds are not particularly restricted but may beany of phosphorus-containing compounds, and there may be mentioned, forexample, phosphoric acids such as orthophosphoric acid, metaphosphoricacid, pyrophosphoric acid, triphosphoric acid and tetraphosphoric acid;phosphonic acids such as aminotri(methylenephosphonic acid),1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediaminetetra(methylenephosphonic acid) and diethylenetriaminepenta(methylenephosphonic acid); organophosphoric acids such as phytic acid;salts thereof; and the like. These may be used singly or two or more ofthem may be used in combination.

The niobium compounds are not particularly restricted but may be any ofniobium-containing compounds, and there may be mentioned, for example,niobium oxide, niobic acid and salts thereof, fluoroniobic acid salts,fluorooxoniobic acid salts, and the like. These may be used singly ortwo or more of them may be used in combination.

The content of the inorganic corrosion inhibitor (D) is preferably 10%by weight (lower limit) to 40% by weight (upper limit) in thepost-treatment coating. When it is less than 10% by weight, the progressof corrosion may not be inhibited and, if it exceeds 40% by weight, thecoating adhesion may become decreased. The lower limit is morepreferably 15% by weight, and the upper limit is more preferably 35% byweight.

In the post-treatment coating, there may further incorporated one ormore additives, such as pigments, dyes, surfactants and lubricants.Usable as the pigments are inorganic pigments, such as zinc oxide (ZnO)and carbon black, organic color pigments and the like, for instance. Asthe surfactants, there may be mentioned nonionic surfactants, anionicsurfactants and the like, for instance. Usable as the lubricants are,for example, polyethylene waxes, modified polyethylene waxes,tetrafluoroethylene resins and the like.

The post-treatment coating is formed to attain a coating weight of 0.01g/m² (lower limit) to 1 g/m² (upper limit). If the coating weight isless than 0.01 g/m², no improvement may be produced in corrosionresistance after alkaline degreasing and/or in coating adhesion. When itexceeds 1 g/m², the electric conductivity will lower, which may disturbthe weldability and/or electrodeposition coating process. The lowerlimit is more preferably 0.03 g/m², and the upper limit is morepreferably 0.7 g/m².

The post-treatment coating can be formed by applying the post-treatmentcomposition to the zinc-plated steel sheet having the zinc phosphatecoating formed thereon. The method of application is not particularlyrestricted but there may be mentioned, for example, roll coating, airspraying, airless spraying, dipping and the like. Preferably, thesubstrate to be coated is heated in advance or the substrate aftercoating is heated and dried so that the degree of crosslinking of thecoating formed from the post-treatment composition may be increased. Inheating the substrate, the peak metal temperature is preferably withinthe range of 50° C. (lower limit) to 250° C. (upper limit). The lowerlimit is preferably 70° C., and the upper limit is preferably 200° C.When the peak metal temperature is less than 50° C., the rate of waterevaporation is slow, hence no sufficient level of film formability willbe obtained and the solvent resistance and alkali resistance willdecrease. When, conversely, it exceeds 250° C., the resin will bethermally decomposed, and the solvent resistance and alkali resistancewill decrease.

The zinc-plated steel sheet to be used in producing theinorganic-organic composite-treated zinc-plated steel sheet of theinvention is not particularly restricted but there may be mentioned, forexample, zinc-plated or zinc-based alloy-plated steel sheets obtained byzinc-based electroplating, zinc-based hot dip plating or zinc-basedvapor deposition plating, for instance, such as zinc-plated steelsheets, zinc/nickel-plated steel sheets, zinc/iron-plated steel sheets,zinc/chromium-plated steel sheets, zinc/manganese-plated steel sheets,zinc/aluminum-plated steel sheets, and zinc/magnesium-plated steelsheets.

The inorganic-organic composite-treated zinc-plated steel sheet of theinvention, which is obtained by forming a zinc phosphate coating, in acoating weight of 0.3 to 5 g/m², on the zinc-plated steel sheet surfaceand forming thereon a post-treatment coating, in a coating weight of0.01 to 1 g/m², containing at least one compound (A) selected from thegroup consisting of thiocarbonyl group-containing compounds, sulfidegroup-containing compounds and guanidyl group-containing compounds, anorganic resin (B), a crosslinking agent (C) and an inorganic corrosioninhibitor (D), can have firm and strong coatings formed uniformly allover the surface of the steel sheet. As a result, when theinorganic-organic composite-treated zinc-plated steel sheet of theinvention is further shaped and subjected to alkaline degreasingtreatment, the post-treatment coating formed on the inorganic-organiccomposite-treated zinc-plated steel sheet can be prevented from beingdeteriorated or dissolved upon degreasing treatment. Therefore, theinorganic-organic composite-treated zinc-plated steel sheet of theinvention is excellent in corrosion resistance after alkaline degreasingand in coating adhesion.

Since the inorganic-organic composite-treated zinc-plated steel sheet ofthe invention has the constitution described hereinabove, thezinc-plated steel sheet excellent in such characteristics as corrosionresistance after alkaline degreasing and coating adhesion can beobtained without requiring any chromate. Furthermore, theinorganic-organic composite-treated zinc-plated steel sheet can beproduced by an easy and simple production method and is advantageousfrom the cost viewpoint, and can be appropriately used in such variousfields of application as automobiles, household electric appliances andbuilding materials.

The inorganic-organic composite-treated zinc-plated steel sheet of theinvention is excellent in corrosion resistance after alkaline degreasingand in coating adhesion and therefore can be used in such fields ofapplication as automobiles, household electric appliances and buildingmaterials.

BEST MODE FOR CARRYING OUT THE INVENTION

The following examples illustrate the present invention in furtherdetail. These examples are, however, by no means limitative of the scopeof the invention. In the examples, “part(s)” means “part(s) by weight”,unless otherwise specified.

(Method of Treatment of Zinc-Plated Steel Sheets)

Test sheets were prepared using the original plated sheets specified inTable 1 and subjecting them to alkaline degreasing, and then to zincphosphate treatment and post-treatment.

After surface conditioning treatment using a commercial TiO₂ colloidpreparation, the zinc phosphate treatment was carried out using thebaths prepared as specified in Table 2 by the spraying technique at atemperature of 45° C. for a treatment period of 1 to 10 seconds, furtherfollowed by washing with water and drying.

For the post-treatment, the aqueous treatment compositions containingthe ingredients specified in Table 3 in an amount of 10 parts by weightwas applied using a roll coater. TABLE 1 Designation Steel sheets EG20electro-galvanized steel sheets (Zn coating weight per side 20 g/m²)EG30 electro-galvanized steel sheets (Zn coating weight per side 30g/m²) GI70 hot dip galvanized steel sheets(Zn coating weight per side 70g/m²)

TABLE 2 Concentration in bath, g/l No. Zn Ni Mn Mg PO₄ 1 1.1 0.5 — —10.5 2 0.7 2.8 — 0.1 6.5 3 2.0 4.0 — 22 11.0 4 2.5 2.0 2.5 11 14.0

TABLE 3 No. 1 2 3 4 5 6 7 8 Sodium dimethyldithiocarbamate 2 1 — 1 — 1 2— 1,2-Bis(2-hydroxyethylthio)ethane — 1 — — 2 1 — — 1-o-Tolylbiguanide —— 1.5 1 — — — — Resin Ethylene-methacrylic acid copolymer, 65 52 42 3321 — 77.4 48.7 60% Na-neutralized Acrylic resin (acid value 10) — 13 — —— 65 — — Bisphenol A-based epoxy resin — — 21 — — — — 24.3 Polyurethaneresin (acid value 30) — — — 33 42 — — — Crosslinking agent Glycerolpolyglycidyl ether 2.4 1.9 1.9 1.9 1.9 — — 2.4γ-Glycidoxypropyltrimethoxysilane 4 3.5 4 3.5 3.5 — — 4 γ- — 1 — — — — —— Methacryloxypropyltrimethoxysilane Di-n- 6 6 9 — — — — —butoxybis(triethanolaminato)titanium Cymel 385 (Product of Mitsui Cytec)— — — 6 9 — — — Inorganic Snowtex N (product of Nissan 20 20 18 20 20 2020 20 rust Chemical) preventive Diammonium hydrogen phosphate 0.6 0.60.6 0.6 0.6 0.6 0.6 0.6 Niobium oxide — — 2 — — — — —Numerical values being solid matter mass proportions (%).

EXAMPLES 1 TO 8 AND COMPARATIVE EXAMPLES 1 TO 5

Test sheets were produced according to the conditions (original sheetspecies, zinc phosphate treatment bath, coating weight of the zincphosphate coating, post-treatment composition, coating weight of thepost-treatment coating) specified in Table 4. The original sheets usedwere the EG20 or GI70 sheets specified in Table 1, the zinc phosphatetreatment baths used were the baths Nos. 1 to 3 specified in Table 2 (nozinc phosphate treatment was carried out in Comparative Example 1), andthe post-treatment compositions used were the compositions Nos. 1 to 8specified in Table 3. As for the coating weights after zinc phosphatetreatment, the zinc phosphate coatings were dissolved with chromic acidand the coating weights were calculated based on the differences inweight between before and after dissolution. The post-treatmentcompositions were respectively applied to the sample sheets after zincphosphate treatment, and the coated sheets were dried at a peak metaltemperature of 80° C. and then allowed to stand for cooling. Based onthe differences in weight between before and after application, thecoating weights of the post-treatment coating were calculated.

(Methods of Evaluating Typical Performance Characteristics)

<Corrosion Resistance>

The edges and reverse side of each sample were tape-sealed, and thesample was subjected to Salt spray test (SST, JIS Z 2371). After thelapse of 72 hours, the state of white rust formation was observed. Theevaluation criteria were as follows:

-   -   Excellent: No white rust formation;    -   Fair: Less than 10% covered with white rust;    -   Poor: 10% or more covered with white rust.        <Corrosion Resistance After Degreasing>

The edges and reverse side of each sample were tape-sealed, and thesample was degreased with a commercial alkaline degreasing solution(pH=12.5, 40° C., 1 minute of dipping) and then subjected to SST (JIS Z2371). After the lapse of 72 hours, the state of white rust formationwas observed. The evaluation criteria were as follows:

-   -   Excellent: No white rust formation;    -   Fair: Less than 10% covered with white rust;    -   Poor: 10% or more covered with white rust.        <Coating Adhesion>

Each sample was degreased with a commercial alkaline degreasing solution(pH=10.5, 40° C., 1 minute of dipping) and then coated with a melaminealkyd paint (Superlac 100, product of Nippon Paint Co., Ltd.) to a dryfilm thickness of 30 μm, and baking was carried out at 120° C. for 25minutes. After 24 hours of standing, the sample was immersed in boilingwater for 30 minutes, then taken out, allowed to stand for 1 day, givenlattice pattern cuts at 1-mm intervals, and further drawn to 7 mm indepth by the Erichsen tester, followed by peeling with a adhesive tape.The evaluation criteria were as follows:

-   -   Excellent: No peeling;    -   Fair: Peeling around cuts;    -   Poor: Peeling.

The results of the above evaluations are shown in Table 4. TABLE 4Performance characteristic Corrosion Zinc resistance Coating Zinc-phosphate treatment Post-treatment Corrosion after adhesion platedCoating weight Coating weight resistance, degreasing, secondary steelsheet No. g/m² No. g/m² SST SST bond Example 1 EG20 1 1.5 1 0.25Excellent Excellent Excellent 2 EG20 1 1.5 2 0.25 Excellent ExcellentExcellent 3 EG20 1 1.5 3 0.25 Excellent Excellent Excellent 4 EG20 1 1.54 0.25 Excellent Excellent Excellent 5 EG20 1 1.5 5 0.25 ExcellentExcellent Excellent 6 EG20 2 1 2 0.05 Excellent Excellent Excellent 7GI70 3 0.7 3 0.1 Excellent Excellent Excellent 8 EG20 1 1.5 1 1Excellent Excellent Excellent Comparative 1 EG20 — — 1 0.25 Poor PoorPoor Example 2 EG20 1 1.5 — — Poor Poor Poor 3 EG20 1 1.5 6 0.25 FairPoor Fair 4 EG20 1 1.5 7 0.25 Excellent Poor Poor 5 EG20 1 1.5 8 0.25Poor Poor Excellent

EXAMPLES 9 TO 14 AND COMPARATIVE EXAMPLES 6 TO 8

Test sheets were produced according to the conditions (original sheetspecies, zinc phosphate treatment bath, coating weight of the zincphosphate coating, magnesium/phosphorus weight ratio, amount of Mg,post-treatment composition, coating weight of the post-treatmentcoating) specified in Table 5. The original sheets used were the EG30 orGI70 sheets specified in Table 1, the zinc phosphate treatment bathsused were the baths Nos. 3 and 4 specified in Table 2, and thepost-treatment compositions used were the compositions Nos. 1, 3, 5, 6,7 and 8 specified in Table 3. As for the coating weights andcompositions of the zinc phosphate coatings, the zinc phosphate coatingswere dissolved with chromic acid, quantitations were made by ICPanalysis and calculations were made. The post-treatment compositionswere respectively applied to the sample sheets after zinc phosphatetreatment, and the coated sheets were dried at a peak metal temperatureof 150° C., then cooled with water, dried and allowed to stand. Based onthe differences in weight between before and after application, thecoating weights of the post-treatment coating were calculated.

(Methods of Evaluating Typical Performance Characteristics)

<Corrosion Resistance>

Each sample was tape-sealed at the edges and on the reverse side, givencrosscuts (cuts reaching the steel face) with a cutter and subjected toCyclic corrosion test (CCT). After 15 cycles, the state of red rustformation was observed.

[CCT Conditions]

Each cycle comprised 6 hours of salt spraying (5% NaCl, 35° C.)→3 hoursof drying (50° C., 45% RH)→14 hours of wetting (50° C., 95% RH)→1 hourof drying (50° C., 45% RH). This cycle was repeated.

The evaluation criteria were as follows:

-   -   Excellent: No red rust formation;    -   Fair: Red rust formation from around cuts;    -   Poor: Red rust formation all over the surface.        <Corrosion Resistance After Degreasing>

Each sample was tape-sealed at the edges and on the reverse side, givencrosscuts (cuts reaching the steel face) with a cutter, degreased with acommercial alkaline degreasing solution (pH=12.5, 40° C., 1 minute ofdipping) and then subjected to CCT. After 15 cycles, the state of redrust formation was observed. The CCT conditions were the same as in theabove corrosion resistance evaluation. The evaluation criteria were asfollows:

-   -   Excellent: No red rust formation;    -   Fair: Red rust formation from around cuts;    -   Poor: Red rust formation all over the surface.        <Coating Adhesion>

Each sample was degreased with a commercial alkaline degreasing solution(pH=10.5, 40° C., 1 minute of dipping), and subjected to chemicalconversion treatment for automobiles (SURFDINE 2500 MZL, product ofNippon Paint Co., Ltd.) and then to cationic electrodeposition coatingfor automobiles (V 20, product of Nippon Paint Co., Ltd., 20 μm, 170°C., 20 minutes of baking). After 24 hours of standing, the sample wasimmersed in warm water at 50° C. and, after the lapse of 10 days, takenout, given lattice pattern cuts at 2-mm intervals, and drawn to 7 mm indepth by the Erichsen tester, followed by peeling with a tape. Theevaluation criteria were as follows:

-   -   Excellent: No peeling;    -   Fair: Peeling around cuts;    -   Poor: Peeling.

The results of the above evaluations are shown in Table 5. TABLE 5Performance characteristic Post- Corrosion Zinc phosphate treatmenttreatment resistance Coating Zinc- Coating Amount of Coating Corrosionafter adhesion, plated weight Mg/P Mg weight resistance, degreasing,secondary steel sheet No. g/m² mass ratio mg/m² No. g/m² CCT CCT bondExample  9 EG30 3 1.2 0.28 46 1 0.25 Excellent Excellent Excellent 10EG30 3 0.7 0.27 26 1 0.25 Excellent Excellent Excellent 11 EG30 4 1.40.11 21 3 0.25 Excellent Excellent Excellent 12 GI70 4 1.5 0.11 24 30.25 Excellent Excellent Excellent 13 EG30 4 1.4 0.11 21 5 0.5 ExcellentExcellent Excellent 14 EG30 4 1.4 0.11 21 5 1 Excellent ExcellentExcellent Comparative  6 EG30 4 1.4 0.11 21 6 0.25 Fair Poor PoorExample  7 EG30 4 1.4 0.11 21 7 0.25 Fair Poor Poor  8 EG30 4 1.4 0.1121 8 0.25 Poor Poor Excellent

The test sheets obtained by using EG20 and the zinc phosphate treatmentbaths Nos. 1 and 2 (Examples 1 to 6 and 8) were excellent in therespective performance characteristics. Even when EG30 sheets were used,the use of the zinc phosphate treatment baths Nos. 3 and 4 (Examples 9to 11, 13 and 14) made it possible to obtain coated sheets excellent inthe respective performance characteristics. Further, when GI70 sheetswere used (Examples 7 and 12), coated sheets excellent in the respectiveperformance characteristics could be obtained as well. On the contrary,the test sheets obtained in the comparative examples were not excellentin all of the performance characteristics.

1. An inorganic-organic composite-treated zinc-plated steel sheet whichhas a zinc phosphate coating, in a coating weight of 0.3 to 5 g/m², onthe zinc-plated steel sheet surface and, thereon, a post-treatmentcoating, in a coating weight of 0.01 to 1 g/m², containing at least onecompound (A) selected from the group consisting of thiocarbonylgroup-containing compounds, sulfide group-containing compounds andguanidyl group-containing compounds, an organic resin (B), acrosslinking agent (C) and an inorganic corrosion inhibitor (D).
 2. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 1, wherein said zinc phosphate coating contains magnesium, themagnesium/phosphorus (weight ratio) in said zinc phosphate coating beingnot less than 0.1 and the amount of magnesium being not less than 20mg/m².
 3. The inorganic-organic composite-treated zinc-plated steelsheet according to claim 1, wherein said post-treatment coating has thefollowing composition: 0.1 to 10% by weight of at least one compound.(A) selected from the group consisting of thiocarbonyl group-containingcompounds, sulfide group-containing compounds and guanidylgroup-containing compounds, 40 to 80% by weight of the organic resin(B), 5 to 30% by weight of the crosslinking agent (C) and 10 to 40% byweight of the inorganic corrosion inhibitor (D).
 4. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 1, wherein said organic resin (B) comprises a neutralizedethylene-unsaturated carboxylic acid copolymer (B1) and at least oneresin (B2) selected from the group consisting of acrylic resins,polyester resins, polyurethane resins and epoxy resins, said copolymer(B1) having a degree of neutralization with an alkali metal of 30 to90%, said resin (B2) having at least one functional group selected fromthe group consisting of carboxyl, hydroxyl and amide groups, and theweight ratio between said copolymer (B1) and said resin (B2) being 100:0to 20:80.
 5. The inorganic-organic composite-treated zinc-plated steelsheet according to claim 1, wherein said crosslinking agent (C) is atleast one species selected from the group consisting of epoxy compounds,silane compounds, organic titanium compounds, amino resins, blockedisocyanate compounds and carbodiimide compounds.
 6. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 1, wherein said inorganic corrosion inhibitor (D) is at least onespecies selected from the group consisting of silica particles,phosphoric acid compounds and niobium compounds.
 7. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 2, wherein said post-treatment coating has the followingcomposition: 0.1 to 10% by weight of at least one compound (A) selectedfrom the group consisting of thiocarbonyl group-containing compounds,sulfide group-containing compounds and guanidyl group-containingcompounds, 40 to 80% by weight of the organic resin (B), 5 to 30% byweight of the crosslinking agent (C) and 10 to 40% by weight of theinorganic corrosion inhibitor (D).
 8. The inorganic-organiccomposite-treated zinc-plated steel sheet according to claim 2, whereinsaid organic resin (B) comprises a neutralized ethylene-unsaturatedcarboxylic acid copolymer (B1) and at least one resin (B2) selected fromthe group consisting of acrylic resins, polyester resins, polyurethaneresins and epoxy resins, said copolymer (B1) having a degree ofneutralization with an alkali metal of 30 to 90%, said resin (B2) havingat least one functional group selected from the group consisting ofcarboxyl, hydroxyl and amide groups, and the weight ratio between saidcopolymer (B1) and said resin (B2) being 100:0 to 20:80.
 9. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 3, wherein said organic resin (B) comprises a neutralizedethylene-unsaturated carboxylic acid copolymer (B1) and at least oneresin (B2) selected from the group consisting of acrylic resins,polyester resins, polyurethane resins and epoxy resins, said copolymer(B1) having a degree of neutralization with an alkali metal of 30 to90%, said resin (B2) having at least one functional group selected fromthe group consisting of carboxyl, hydroxyl and amide groups, and theweight ratio between said copolymer (B1) and said resin (B2) being 100:0to 20:80.
 10. The inorganic-organic composite-treated zinc-plated steelsheet according to claim 2, wherein said crosslinking agent (C) is atleast one species selected from the group consisting of epoxy compounds,silane compounds, organic titanium compounds, amino resins, blockedisocyanate compounds and carbodiimide compounds.
 11. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 3, wherein said crosslinking agent (C) is at least one speciesselected from the group consisting of epoxy compounds, silane compounds,organic titanium compounds, amino resins, blocked isocyanate compoundsand carbodiimide compounds.
 12. The inorganic-organic composite-treatedzinc-plated steel sheet according to claim 4, wherein said crosslinkingagent (C) is at least one species selected from the group consisting ofepoxy compounds, silane compounds, organic titanium compounds, aminoresins, blocked isocyanate compounds and carbodiimide compounds.
 13. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 2, wherein said inorganic corrosion inhibitor (D) is at least onespecies selected from the group consisting of silica particles,phosphoric acid compounds and niobium compounds.
 14. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 3, wherein said inorganic corrosion inhibitor (D) is at least onespecies selected from the group consisting of silica particles,phosphoric acid compounds and niobium compounds.
 15. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 4, wherein said inorganic corrosion inhibitor (D) is at least onespecies selected from the group consisting of silica particles,phosphoric acid compounds and niobium compounds.
 16. Theinorganic-organic composite-treated zinc-plated steel sheet according toclaim 5, wherein said inorganic corrosion inhibitor (D) is at least onespecies selected from the group consisting of silica particles,phosphoric acid compounds and niobium compounds.